Product Recalls in Nevada
Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,659 recalls have been distributed to Nevada in the last 12 months.
Showing 10861–10880 of 50,223 recalls
Recalled Item: ASTUTE REAGENT ASTUTE ELECTRONIC QUALITY CTRL DEVICE US Recalled by...
The Issue: As the temperature and time out of range was exceeded, product performances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST CLINICAL CEFTOLOZANE/TAZO C/T US S30 Recalled by Biomerieux Inc Due to...
The Issue: As the temperature and time out of range was exceeded, product performances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 REAGENT AST-GN73 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...
The Issue: As the temperature and time out of range was exceeded, product performances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DCOUNT SYSTEMS REAGENTS CHEMCHROME V14 (6X1.8ML) Recalled by Biomerieux Inc...
The Issue: As the temperature and time out of range was exceeded, product performances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API 20 E 25 STRIPS Recalled by Biomerieux Inc Due to As the temperature and...
The Issue: As the temperature and time out of range was exceeded, product performances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS CLINICAL VIDAS PROGESTERONE 60 TESTS Recalled by Biomerieux Inc Due to...
The Issue: As the temperature and time out of range was exceeded, product performances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API STAPH 25 STRIPS+25 MEDIA Recalled by Biomerieux Inc Due to As the...
The Issue: As the temperature and time out of range was exceeded, product performances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InPen Diabetes Management App Recalled by Companion Medical, Inc. Due to...
The Issue: Diabetes management app may crash immediately upon opening, while using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD Recalled by Corin Ltd Due to The BIOLOX Delta...
The Issue: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9 Gauge Disposable Trocars with Blunt Pushers for Use with Recalled by ENDO...
The Issue: No expiration dates printed on the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD Recalled by Corin Ltd Due to The BIOLOX Delta...
The Issue: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne CDx (F1CDx) Recalled by Foundation Medicine, Inc. Due to...
The Issue: Reports were sent to customers without the companion diagnostic (CDx) Claims...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne Liquid CDx (F1LCDx) Recalled by Foundation Medicine, Inc. Due...
The Issue: Reports were sent to customers without the companion diagnostic (CDx) Claims...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Angiographic Catheter Extensions. Used to transport fluid from the...
The Issue: There is a potential for separation at the male connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System...
The Issue: The power backup battery, under certain conditions, may exhibit reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control...
The Issue: For one lot of CBC-3D Hematology Control, the Normal Level may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betty Buzz Sparkling Grapefruit - Non-alcoholic Beverage & Mixer Container...
The Issue: Beverage has off-odor
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...
The Issue: Chemical Contamination: FDA analysis found 1 lot of Adam's Polishes ALCOHOL...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...
The Issue: CGMP Deviations: Other lots of hand sanitizer are being recalled because...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HF Resection Electrodes Recalled by Olympus Corporation of the Americas Due...
The Issue: An incompatible HF cable may be packaged with the HF Resection Electrodes....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.